Senior Director, Supply Chain

ORIC is a research-driven company dedicated to discovering and developing novel therapies that can Overcome Resistance In Cancer. Our collaborative, empowering culture gives scientists authority, responsibility, and support to do cutting-edge work on therapies for treatment-resistant cancers. Reporting to the Chief Technical Officer (CTO), the Senior Director, Supply Chain will lead clinical supply chain team operations and commercial supply chain planning. This individual will lead the clinical supply chain team and manage end-to-end clinical supply activities for clinical stage programs and plan to commercialize late-stage assets. Job Description Responsibilities include and are not limited to the following: Develop comprehensive, strategic clinical and commercial supply chain plans and manage operational budgets. Manage external consultants and third-party vendors, including collaborating with QA on vendor selection and quality and supplier agreement development. Interpret clinical trial drug requests and protocols and develop clinical packaging strategies, timelines, and budgets. Responsible for scheduling and delivery of clinical supplies, including creating label and packaging design, subject randomization, packaging, labelling and distribution of clinical supplies. Responsible for establishing a cost-effective and efficient commercial labeling and distribution system. Coordinate primary and secondary packaging, labeling, testing, distribution and return drug management activities with CMO’s. Demonstrate a high level of adaptability in dynamic and fast-paced environments. Operate closely with logistics function to proactively plan, document, and facilitate global cross border distribution strategies. Interface with QA, RA, CMC/manufacturing to ensure trial supplies are appropriately supported. Develop and manage forecasting and ordering investigational product, commercial and comparator material in global trials. Proactively find solutions to emerging issues in an effective manner while taking into consideration risks and cost-effectiveness. Independently create clinical supply study budgets and monitor spend to-date compared to the approved study budget. Develop new functional SOPs, Policies/Plans as necessary. Exhibit leadership capabilities to manage and develop Clinical Supply Managers of all experience levels. Qualifications Required Qualifications: 15+ years of relevant experience in clinical and commercial supply chain management in the pharmaceutical industry with an MA/MBA or equivalent desired. Proficiency in ICH, GMP, and regulatory guidance important to new drug development and commercialization. Demonstrated success in working with and managing CDMOs and external partners using succinct and thorough communication skills. Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment. Demonstrated initiative, ownership, problem identification, problem solving, and analytical and strategic thinking skills. Results driven, collaborative leader with proven ability to perform in a fast-paced environment with a high attention to detail. Excellent verbal and written communication skills, with the ability to build productive long-term team relationships at all levels of supplier organizations. ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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